Canonical Allele Identifier: CA345736935

Gene: RNASEH1

Linked Data

• MyVariant Identifiers: chr2:g.3596677G>C (hg19) ; chr2:g.3549087G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.3549087G>C , CM000664.2:g.3549087G>C	GRCh38
NC_000002.11:g.3596677G>C , CM000664.1:g.3596677G>C	GRCh37
NC_000002.10:g.3574552G>C	NCBI36
NG_051310.1:g.14285C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315212.4:c.535C>G MANE Select	ENSP00000313350.3:p.Arg179Gly
ENST00000654051.1:c.535C>G	ENSP00000499604.1:p.Arg179Gly
ENST00000658393.1:c.535C>G	ENSP00000499330.1:p.Arg179Gly
ENST00000315212.3:c.535C>G	ENSP00000313350.3:p.Arg179Gly
ENST00000436842.5:c.*641C>G	ENSP00000404926.1:n.*641C>G
NM_001286834.1:c.457C>G	NP_001273763.1:p.Arg153Gly
NM_001286837.1:c.184C>G	NP_001273766.1:p.Arg62Gly
NM_002936.4:c.535C>G	NP_002927.2:p.Arg179Gly
XR_244873.1:n.642C>G
XR_922665.1:n.642C>G
XR_922666.1:n.642C>G
XR_922667.1:n.642C>G
XR_922668.1:n.642C>G
XR_922669.1:n.642C>G
XR_922670.1:n.642C>G
XR_922671.1:n.642C>G
XR_922672.1:n.642C>G
XR_922673.1:n.642C>G
XR_922674.1:n.642C>G
NM_001286834.2:c.457C>G	NP_001273763.1:p.Arg153Gly
NM_001286837.2:c.184C>G	NP_001273766.1:p.Arg62Gly
NM_002936.5:c.535C>G	NP_002927.2:p.Arg179Gly
NR_148532.1:n.646C>G
NR_148533.1:n.646C>G
NR_148534.1:n.646C>G
NM_001286837.3:c.184C>G	NP_001273766.1:p.Arg62Gly
NR_148532.2:n.608C>G
NR_148533.2:n.608C>G
NR_148534.2:n.608C>G
NM_001286834.3:c.457C>G	NP_001273763.1:p.Arg153Gly
NM_001378271.1:c.535C>G	NP_001365200.1:p.Arg179Gly
NM_001378272.1:c.532C>G	NP_001365201.1:p.Arg178Gly
NM_001378273.1:c.520C>G	NP_001365202.1:p.Arg174Gly
NM_002936.6:c.535C>G MANE Select	NP_002927.2:p.Arg179Gly
NR_165465.1:n.492C>G
NR_165466.1:n.583-6C>G
NR_165467.1:n.777C>G
NR_165468.1:n.580C>G